http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-H0984598-A
Outgoing Links
Predicate | Object |
---|---|
assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_4eefac142a032449aa6a1a51fadaf766 |
classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-48 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G01N33-50 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-00 |
filingDate | 1995-09-22-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_8a8046ed7a91ce61ba87154eb7e3dc01 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_9a9aa84653e50706ef7ad846133653bd |
publicationDate | 1997-03-31-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationNumber | JP-H0984598-A |
titleOfInvention | Method and reagent for measuring enzyme activity |
abstract | (57) [Abstract] [Problem] Measuring the absorbance in the wavelength range of 400 to 450 nm, Provided are a method and a reagent for suppressing an error in a measured value generated when measuring an enzyme activity in a sample and obtaining a more accurate measured value. SOLUTION: The influence of hemoglobin is avoided by mixing a synthetic substrate reagent containing sodium disulfite with a sample and then measuring the change in absorbance of the resulting mixture in the wavelength range of 400 to 450 nm. Accurately measure the γ-glutamyltransferase activity in the sample. |
isCitedBy | http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-7407774-B2 |
priorityDate | 1995-09-22-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 30.